Scholay

学术搜索 · AI 审稿 · LaTeX 协作

Phase II Study of Picoplatin As Second-Line Therapy for Patients With Small-Cell Lung Cancer

作者:John Randall Eckardt, Dmitry Bentsion, Oleg Nikolaevich Lipatov, Igor S. Polyakov, Frederick R. MacKintosh, David Alan Karlin, Gizelle S. Baker, Hazel B. Breitz · 发表于:Journal of Clinical Oncology · 年份:2009 · DOI:10.1200/jco.2008.19.3235 · 被引用次数:92 · 研究领域:Lung Cancer Research Studies、Lung Cancer Treatments and Mutations、Cancer Treatment and Pharmacology

PURPOSE: This study was designed to confirm the efficacy and safety of picoplatin, a cisplatin analog designed to overcome platinum resistance, in patients with small-cell lung cancer (SCLC) with platinum-refractory/-resistant disease. PATIENTS AND METHODS: All patients received intravenous picoplatin 150 mg/m(2) every 3 weeks. Tumor response, progression-free survival, and overall survival were evaluated. Adverse events were assessed for frequency, severity, and relationship to treatment. Quality of life was assessed with the Lung Cancer Symptom Scale instrument. RESULTS: Seventy-seven patients were treated with picoplatin (median number of cycles, two; range one to 10). Three patients (4%) had a partial response, 33 (43%) had stable disease (four of these were unconfirmed partial responses), 36 (47%) had progressive disease, and five were not assessable for response. Median progression-free survival was 9.1 weeks (95% CI, 7.0 to 12.1 weeks). Median overall survival was 26.9 weeks (95% CI, 21.1 to 33.4). The most common grade 3 and 4 toxicities were thrombocytopenia (48%), neutropenia (25%), and anemia (20%). The most commonly reported adverse events of any severity included thrombocytopenia (64%), anemia (49%), neutropenia (39%), nausea (27%), fatigue (16%), and dyspnea (16%). No severe neurotoxicity or nephrotoxicity were observed. There were no treatment-related deaths. CONCLUSION: Picoplatin demonstrated clinical efficacy in platinum-refractory SCLC. The major toxicity w...